Class II — Linkbio Corp.
| Recalling firm | LinkBio Corp. |
|---|---|
| Registered facility | LinkBio Corp. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen. |
| Product | LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136. |
| Quantity | 5 units |
| Distribution | US Nationwide distribution in the state of Alabama, Florida, and Kansas. |
| Initiated | 2026-03-12 |
| Classified | 2026-04-10 |
| Recall number | Z-1810-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Linkbio Corp. (Z-1810-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/98594/
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